← Back to catalogue

Quickie Q700-UP M / Q700M

FDA UDIEUDAMED

Class II (US FDA UDI)

by Sunrise Medical (US) LLC

Identity

Trade Name
Quickie Q700-UP M / Q700M FDA UDI
Generic Name
Electric-motor-driven wheelchair, occupant-controlled FDA UDI
Device Name
Power wheelchair, midwheel drive with or without stand-up feature. Q700-UP M / Q700M. ERGO/PRO FDA UDI
Model / Reference
Q700-UP M / Q700M FDA UDI
Description
Power wheelchair, midwheel drive with or without stand-up feature. Q700-UP M / Q700M. ERGO/PRO FDA UDI

Identifiers

Catalog Number
EIPW25 FDA UDI
Primary DI / UDI-DI
00016958059793 FDA UDI
FDA Product Code
IPL FDA UDI
ITI FDA UDI
GMDN Term
Electric-motor-driven wheelchair, occupant-controlled FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3900 FDA UDI
890.3860 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electric-motor-driven wheelchair, occupant-controlled

Quickie Q700-UP M / Q700M by Sunrise Medical (US) LLC — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Electric-motor-driven wheelchair, occupant-controlled.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (2)

  • FDA UDI 1e028f6b-72f1-4cf4-a560-36c1ba0cd911 34 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced Jun 4, 2026